regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ADAM32_chr8_39102734_39289917 | 39142110 | GA | G | intron_variant | MODIFIER | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0005 | a0001c0001t0001a0002c0005t0001 | a0001c0001t0001g0002a0001c0001t0001g0251a0001c0001t0001g0252others(2): Show | 6 | 257 | 0.0234 | -1 | c.201 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39145041 | GA | G | intron_variant | MODIFIER | HG02723.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
a0002a0005a0007 | a0002c0003a0005c0006a0007c0009 | a0002c0003t0001a0005c0006t0001a0007c0009t0001 | a0002c0003t0001g0150a0005c0006t0001g0143a0005c0006t0001g0215others(3): Show | 6 | 257 | 0.0234 | -1 | c.201 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39148481 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0002a0002c0003others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(17): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 257 | 257 | 1.0000 | -1 | c.276 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39152720 | CA | C | intron_variant | MODIFIER | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(16): Show |
a0001a0002a0006others(1): Show | a0001c0001a0002c0003a0002c0005others(2): Show | a0001c0001t0001a0001c0001t0002a0002c0003t0001others(4): Show | a0001c0001t0001g0148a0001c0001t0001g0176a0001c0001t0001g0240others(16): Show | 19 | 257 | 0.0739 | -1 | c.525 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39160539 | CA | C | intron_variant | MODIFIER | HG00423.hp2 HG01175.hp1 HG01192.hp2 others(9): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(1): Show | a0001c0001t0001g0200a0001c0001t0001g0214a0001c0001t0001g0218others(9): Show | 12 | 257 | 0.0467 | -1 | c.526 others(8): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39162707 | TA | T | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(76): Show |
a0001a0002a0007others(2): Show | a0001c0001a0001c0002a0002c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(7): Show | a0001c0001t0001g0007a0001c0001t0002g0127a0001c0001t0002g0128others(75): Show | 79 | 257 | 0.3074 | -1 | c.594 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39173780 | GT | G | intron_variant | MODIFIER | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(2): Show |
a0004a0011 | a0004c0007a0011c0013 | a0004c0007t0001a0011c0013t0001 | a0004c0007t0001g0153a0004c0007t0001g0154a0004c0007t0001g0155others(2): Show | 5 | 257 | 0.0195 | -1 | c.915 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39174467 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(156): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0002c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(10): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 159 | 257 | 0.6187 | -1 | c.915 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39177061 | CT | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(75): Show |
a0001a0002a0007others(2): Show | a0001c0001a0001c0002a0002c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(7): Show | a0001c0001t0001g0007a0001c0001t0002g0127a0001c0001t0002g0128others(74): Show | 78 | 257 | 0.3035 | -1 | c.915 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39177761 | GT | G | intron_variant | MODIFIER | HG00408.hp2 HG00621.hp2 HG00735.hp1 others(27): Show |
a0001a0002a0003 | a0001c0001a0002c0003a0002c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0002c0003t0002others(2): Show | a0001c0001t0001g0002a0001c0001t0001g0149a0001c0001t0001g0234others(26): Show | 30 | 257 | 0.1167 | -1 | c.915 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39185265 | CA | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0002a0002c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(14): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(234): Show | 239 | 257 | 0.9300 | -1 | c.916 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39191600 | GT | G | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(78): Show |
a0001a0002a0007others(2): Show | a0001c0001a0001c0002a0002c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(7): Show | a0001c0001t0001g0007a0001c0001t0002g0030a0001c0001t0002g0127others(77): Show | 81 | 257 | 0.3152 | -1 | c.105 others(10): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39198739 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
a0001a0002a0006others(3): Show | a0001c0001a0001c0002a0002c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(9): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(183): Show | 187 | 257 | 0.7276 | -1 | c.105 others(11): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39200453 | CA | C | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(155): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0002c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(10): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(154): Show | 158 | 257 | 0.6148 | -1 | c.105 others(11): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39202937 | TG | T | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(155): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0002c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(10): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(154): Show | 158 | 257 | 0.6148 | -1 | c.105 others(10): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39212571 | TA | T | intron_variant | MODIFIER | HG02976.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0001 | a0001c0001t0001g0007a0002c0003t0001g0156a0002c0003t0001g0253others(1): Show | 4 | 257 | 0.0156 | -1 | c.123 others(10): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39220964 | TC | T | intron_variant | MODIFIER | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(17): Show |
a0001a0002a0007 | a0001c0001a0002c0003a0002c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0002c0003t0001others(3): Show | a0001c0001t0001g0148a0001c0001t0001g0176a0001c0001t0001g0209others(17): Show | 20 | 257 | 0.0778 | -1 | c.123 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 12/24 | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39223632 | AT | A | intron_variant | MODIFIER | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(12): Show |
a0003a0005a0012 | a0003c0004a0005c0006a0012c0011 | a0003c0004t0001a0003c0004t0002a0005c0006t0001others(1): Show | a0003c0004t0001g0133a0003c0004t0001g0134a0003c0004t0001g0135others(12): Show | 15 | 257 | 0.0584 | -1 | c.152 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39247778 | GT | G | intron_variant | MODIFIER | HG00639.hp2 HG00735.hp2 HG01175.hp1 others(16): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0001c0001t0002a0002c0003t0001 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0182others(16): Show | 19 | 257 | 0.0739 | -1 | c.190 others(10): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39247895 | CT | C | intron_variant | MODIFIER | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(17): Show |
a0002a0003a0004others(4): Show | a0002c0003a0003c0004a0004c0007others(4): Show | a0002c0003t0001a0003c0004t0001a0003c0004t0002others(5): Show | a0002c0003t0001g0150a0003c0004t0001g0133a0003c0004t0001g0134others(17): Show | 20 | 257 | 0.0778 | -1 | c.190 others(10): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39251378 | CA | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(98): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0002a0002c0003others(8): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(11): Show | a0001c0001t0001g0248a0001c0002t0001g0145a0001c0002t0001g0147others(97): Show | 101 | 257 | 0.3930 | -1 | c.190 others(10): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39252405 | CA | C | intron_variant | MODIFIER | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
a0005 | a0005c0006 | a0005c0006t0001 | a0005c0006t0001g0143a0005c0006t0001g0215a0005c0006t0001g0221 | 3 | 257 | 0.0117 | -1 | c.190 others(10): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39254225 | CT | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(85): Show |
a0001a0002a0005others(3): Show | a0001c0001a0001c0002a0002c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(8): Show | a0001c0001t0001g0248a0001c0001t0002g0028a0001c0002t0001g0145others(84): Show | 88 | 257 | 0.3424 | -1 | c.190 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39257157 | GT | G | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(77): Show |
a0001a0002a0008 | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(4): Show | a0001c0001t0001g0248a0001c0002t0001g0145a0001c0002t0001g0147others(76): Show | 80 | 257 | 0.3113 | -1 | c.200 others(8): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39258395 | TA | T | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(119): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0002a0002c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(14): Show | a0001c0001t0001g0148a0001c0001t0001g0176a0001c0001t0001g0209others(118): Show | 122 | 257 | 0.4747 | -1 | c.216 others(10): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39262204 | GT | G | intron_variant | MODIFIER | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
a0003a0012 | a0003c0004a0012c0011 | a0003c0004t0001a0003c0004t0002a0012c0011t0001 | a0003c0004t0001g0133a0003c0004t0001g0134a0003c0004t0001g0135others(8): Show | 11 | 257 | 0.0428 | -1 | c.216 others(10): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39270991 | AT | A | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(74): Show |
a0001a0002a0008 | a0001c0002a0002c0005a0008c0014 | a0001c0002t0001a0001c0002t0002a0002c0005t0001others(2): Show | a0001c0002t0001g0145a0001c0002t0001g0147a0001c0002t0001g0161others(73): Show | 77 | 257 | 0.2996 | -1 | c.220 others(8): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39271460 | CA | C | intron_variant | MODIFIER | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(48): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0001c0001t0002a0002c0003t0001others(1): Show | a0001c0001t0001g0002a0001c0001t0001g0148a0001c0001t0001g0149others(47): Show | 51 | 257 | 0.1984 | -1 | c.220 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39271539 | CA | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(89): Show |
a0001a0002a0008 | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(5): Show | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0182others(88): Show | 92 | 257 | 0.3580 | -1 | c.220 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39272101 | GA | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0002a0002c0003others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(17): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(246): Show | 251 | 257 | 0.9767 | -1 | c.220 others(10): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39273803 | AT | A | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
a0001a0002a0008 | a0001c0002a0002c0005a0008c0014 | a0001c0002t0001a0001c0002t0002a0002c0005t0001others(2): Show | a0001c0002t0001g0145a0001c0002t0001g0147a0001c0002t0001g0161others(72): Show | 76 | 257 | 0.2957 | -1 | c.220 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39274018 | GT | G | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(115): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0002a0002c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(14): Show | a0001c0001t0001g0148a0001c0001t0001g0176a0001c0001t0001g0209others(114): Show | 118 | 257 | 0.4591 | -1 | c.220 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39276297 | GA | G | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(76): Show |
a0001a0002a0008 | a0001c0002a0002c0003a0002c0005others(1): Show | a0001c0002t0001a0001c0002t0002a0002c0003t0001others(3): Show | a0001c0002t0001g0145a0001c0002t0001g0147a0001c0002t0001g0161others(75): Show | 79 | 257 | 0.3074 | -1 | c.227 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39281013 | AC | A | intron_variant | MODIFIER | HG03225.hp1 HG03486.hp1 NA20300.hp2 |
a0002a0005 | a0002c0003a0005c0006 | a0002c0003t0001a0005c0006t0001 | a0002c0003t0001g0164a0002c0003t0001g0165a0005c0006t0001g0222 | 3 | 257 | 0.0117 | -1 | c.228 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39283411 | TA | T | intron_variant | MODIFIER | HG00280.hp2 HG02895.hp2 NA19074.hp1 others(2): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0002t0002others(1): Show | a0001c0001t0001g0157a0001c0001t0002g0079a0001c0001t0002g0080others(2): Show | 5 | 257 | 0.0195 | -1 | c.231 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39283771 | CT | C | intron_variant | MODIFIER | HG02895.hp2 HG02896.hp1 HG02897.hp2 others(5): Show |
a0001a0002a0003 | a0001c0002a0002c0003a0002c0005others(1): Show | a0001c0002t0002a0002c0003t0001a0002c0005t0002others(1): Show | a0001c0002t0002g0090a0002c0003t0001g0150a0002c0003t0001g0156others(5): Show | 8 | 257 | 0.0311 | -1 | c.235 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM32_chr8_39102734_39289917 | 39285476 | AC | A | downstream_gene_variant | MODIFIER | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(1): Show |
a0004 | a0004c0007 | a0004c0007t0001 | a0004c0007t0001g0153a0004c0007t0001g0154a0004c0007t0001g0155others(1): Show | 4 | 257 | 0.0156 | -1 | c.*67 others(5): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 560 | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39285625 | GT | G | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00408.hp2 HG01169.hp2 others(12): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(3): Show | a0001c0001t0001g0170a0001c0001t0001g0174a0001c0001t0002g0020others(12): Show | 15 | 257 | 0.0584 | -1 | c.*82 others(5): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 709 | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39285660 | CG | C | downstream_gene_variant | MODIFIER | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(26): Show |
a0001a0008 | a0001c0001a0001c0002a0008c0014 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(2): Show | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0201others(26): Show | 29 | 257 | 0.1128 | -1 | c.*86 others(5): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 744 | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39286739 | CT | C | downstream_gene_variant | MODIFIER | HG00735.hp1 HG01943.hp1 HG02015.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0002t0001 | a0001c0001t0001g0252a0001c0001t0002g0019a0001c0001t0002g0022others(2): Show | 5 | 257 | 0.0195 | -1 | c.*19 others(6): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1823 | chr8 | TogoVar | ||||||
ADAM33_chr20_3662975_3687010 | 3666741 | CT | C | downstream_gene_variant | MODIFIER | HG00140.hp2 HG00323.hp1 HG00673.hp1 others(32): Show |
a0000a0001a0002others(4): Show | a0000c0003a0001c0001a0001c0006others(6): Show | a0000c0003t0007a0000c0003t0008a0001c0001t0001others(11): Show | a0000c0003t0007g0270a0000c0003t0008g0240a0001c0001t0001g0272others(30): Show | 35 | 462 | 0.0758 | -1 | c.*22 others(6): Show |
ADAM33 | ENSG00000149451.19 | transcript | ENST00000356518.7 | protein_coding | 1233 | chr20 | TogoVar | ||||||
ADAM33_chr20_3662975_3687010 | 3676418 | CT | C | intron_variant | MODIFIER | HG00140.hp2 HG00733.hp2 HG02257.hp2 others(7): Show |
a0001 | a0001c0001a0001c0012 | a0001c0001t0001a0001c0001t0003a0001c0001t0013others(1): Show | a0001c0001t0001g0014a0001c0001t0001g0061a0001c0001t0001g0192others(6): Show | 10 | 462 | 0.0217 | -1 | c.254 others(8): Show |
ADAM33 | ENSG00000149451.19 | transcript | ENST00000356518.7 | protein_coding | 3/21 | chr20 | TogoVar | ||||||
ADAM33_chr20_3662975_3687010 | 3679136 | CT | C | intron_variant | MODIFIER | HG00597.hp1 HG01516.hp2 HG01517.hp1 others(14): Show |
a0000a0001a0003others(3): Show | a0000c0003a0000c0013a0001c0001others(6): Show | a0000c0003t0007a0000c0013t0021a0000c0013t0036others(8): Show | a0000c0003t0007g0249a0000c0013t0021g0065a0000c0013t0036g0064others(14): Show | 17 | 462 | 0.0368 | -1 | c.177 others(8): Show |
ADAM33 | ENSG00000149451.19 | transcript | ENST00000356518.7 | protein_coding | 2/21 | chr20 | TogoVar | ||||||
ADAM33_chr20_3662975_3687010 | 3683125 | CT | C | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00323.hp1 HG01069.hp1 others(48): Show |
a0000a0001a0002others(5): Show | a0000c0003a0000c0009a0000c0010others(11): Show | a0000c0003t0007a0000c0009t0007a0000c0010t0031others(17): Show | a0000c0003t0007g0140a0000c0009t0007g0007a0000c0009t0007g0090others(42): Show | 51 | 462 | 0.1104 | -1 | c.-11 others(6): Show |
ADAM33 | ENSG00000149451.19 | transcript | ENST00000356518.7 | protein_coding | 1116 | chr20 | TogoVar | ||||||
ADAM33_chr20_3662975_3687010 | 3683702 | CT | C | upstream_gene_variant | MODIFIER | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(87): Show |
a0000a0001a0002others(5): Show | a0000c0003a0000c0009a0000c0013others(18): Show | a0000c0003t0007a0000c0003t0008a0000c0003t0032others(32): Show | a0000c0003t0007g0197a0000c0003t0007g0241a0000c0003t0007g0249others(77): Show | 90 | 462 | 0.1948 | -1 | c.-16 others(6): Show |
ADAM33 | ENSG00000149451.19 | transcript | ENST00000356518.7 | protein_coding | 1693 | chr20 | TogoVar | ||||||
ADAM33_chr20_3662975_3687010 | 3683956 | AG | A | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(457): Show |
a0000a0001a0002others(17): Show | a0000c0003a0000c0009a0000c0010others(43): Show | a0000c0003t0007a0000c0003t0008a0000c0003t0032others(87): Show | a0000c0003t0007g0058a0000c0003t0007g0095a0000c0003t0007g0096others(375): Show | 460 | 462 | 0.9957 | -1 | c.-19 others(6): Show |
ADAM33 | ENSG00000149451.19 | transcript | ENST00000356518.7 | protein_coding | 1947 | chr20 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24440582 | AC | A | upstream_gene_variant | MODIFIER | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
a0001a0016a0017 | a0001c0002a0016c0015a0017c0016 | a0001c0002t0004a0016c0015t0004a0017c0016t0008 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(7): Show | 10 | 360 | 0.0278 | -1 | c.-52 others(5): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 443 | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24446727 | GA | G | intron_variant | MODIFIER | HG02572.hp1 HG02970.hp1 HG03139.hp2 |
a0003 | a0003c0011 | a0003c0011t0001 | a0003c0011t0001g0011a0003c0011t0001g0074 | 3 | 360 | 0.0083 | -1 | c.157 others(8): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24453259 | TC | T | intron_variant | MODIFIER | HG02004.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0027a0001c0002t0001g0206a0001c0002t0001g0207others(1): Show | 5 | 360 | 0.0139 | -1 | c.233 others(9): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM7_chr8_24436026_24514565 | 24456632 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0002a0001c0004others(26): Show | a0001c0001t0002a0001c0001t0009a0001c0001t0010others(34): Show | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0023others(293): Show | 336 | 360 | 0.9333 | -1 | c.234 others(9): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar |